Highly ordered mesoporous carbon/iron porphyrin nanoreactor for the electrochemical reduction of CO2

被引:22
作者
Choi, Jaecheol [1 ]
Kim, Jeonghun [2 ,3 ,4 ]
Wagner, Pawel [1 ]
Na, Jongbeom [2 ,3 ]
Wallace, Gordon G. [1 ]
Officer, David L. [1 ]
Yamauchi, Yusuke [2 ,3 ,5 ,6 ]
机构
[1] Univ Wollongong, Intelligent Polymer Res Inst, ARC Ctr Excellence Electromat Sci, Wollongong, NSW 2522, Australia
[2] Univ Queensland, Sch Chem Engn, Brisbane, Qld 4072, Australia
[3] Univ Queensland, Australian Inst Bioengn & Nanotechnol AIBN, Brisbane, Qld 4072, Australia
[4] Kookmin Univ, Dept Chem, 77 Jeongneung Ro, Seoul 02707, South Korea
[5] Kyung Hee Univ, Dept Plant & Environm New Resources, 1732 Deogyeong Daero, Yongin 446701, Gyeonggi Do, South Korea
[6] Natl Inst Mat Sci NIMS, Int Ctr Mat Nanoarchitecton WPI MANA, Tsukuba, Ibaraki 3050044, Japan
基金
新加坡国家研究基金会;
关键词
OXYGEN REDUCTION; NANOPOROUS CARBON; CATALYSTS; ELECTROREDUCTION; PERFORMANCE; COMPOSITES; CONVERSION; NANOTUBES; DISPERSIONS; VOLTAMMETRY;
D O I
10.1039/d0ta04641h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A variety of carbon materials such as carbon nanotubes and graphene have been widely investigated as conductive substrates to immobilize metal complex-based catalysts for electrocatalytic CO(2)reduction. However, highly ordered mesoporous carbons have received scant attention as substrates for CO(2)reduction electrocatalysts. The unique porous structure of such carbon provides the opportunity to not only house catalytically active materials but also facilitate reactant transport. In this work, we propose a simple approach for immobilization of the highly active and cost-efficient molecular catalyst iron porphyrin, into a highly ordered mesoporous carbon, CMK-3 having a large surface area of 1345 m(2)g(-1)viaa simple vacuum infiltration method. The resulting heterogeneous electrocatalyst (CMK-FeTPP) is utilized for the conversion of aqueous CO(2)into CO with 92.1% faradaic efficiency and a high effective turnover frequency of 3.9 s(-1)at an overpotential of 680 mV. We believe that this new approach has the potential to be widely used to fabricate efficient electrocatalysts for not only CO(2)conversion but also other electrochemical gas conversion systems.
引用
收藏
页码:14966 / 14974
页数:9
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